Canonical Allele Identifier: PA2826064119
Gene: EFHC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 578529
ClinVar RCV Id: RCV003768078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165891.1:p.Tyr447Asp
CA3856078
NM_001172420.2:c.1339T>G